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Walking at NHF’s Annual Meeting

As you look ahead to the next National Hemophilia Foundation (NHF) Annual Meeting, you'll need to plan ahead to fit...

Kathy Gerus-Darbison remembers the silence. It was the silence she received in response to her questions after she was diagnosed...

HIV

Ray Stanhope may be the one in his family with hemophilia, but he’s not the only one who deals with...

Taking Charge, Advocacy

Finding reputable day care is one of a family’s most important decisions. For a family with children who have been...

Family Matters

Although I received my healthcare early in life from the military and didn’t meet another person with hemophilia until I...

As a kid, you probably help out in lots of ways. You pick up your toys around the house for...

HemAware Junior

Longtime rallying cries in the bleeding disorders community have been for insurance plans to cover all factor products and for...

Insurance

In each issue of HemAware, we “Take 5” with people in the bleeding disorders community and spotlight their accomplishments with...

My Journey

On April 14, 2008, The New York Times reported that there is a new tier of drug coverage in the...

Insurance

In January 2009, the US Food and Drug Administration (FDA) approved CSL Behring’s RiaSTAP™ for the treatment of acute bleeding...

Bob Stribula, 59, has been biking for about half a century. He has no plans to stop. From spring through...

Kody Schrimshaw’s morning routine is usually the same. The 15-year-old high school freshman, who has severe hemophilia A, wakes up...

Generation Next